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Clinical Trial Summary

The purpose of this study is to assess the safety, pharmacokinetics, and immunogenicity of tiragolumab and atezolizumab intravenous fixed-dose combination (IV FDC) in participants with histologically confirmed PD-L1-selected solid tumors whose disease is locally advanced, recurrent, or metastatic and for whom an investigational agent in combination with an anti-PD-L1 antibody is considered an acceptable treatment option.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05661578
Study type Interventional
Source Hoffmann-La Roche
Contact Reference Study ID Number: GO44096 https://forpatients.roche.com
Phone 888-662-6728 (U.S. Only)
Email global-roche-genentech-trials@gene.com
Status Recruiting
Phase Phase 2
Start date May 4, 2023
Completion date February 14, 2025